Abstract
Hexaol host compounds that include guest molecules in a maximum host-to-guest
ratio of 1:6 were prepared. The aromatic hexaol host, hexahydroxytriphenylene,
was found to form a chiral inclusion-complex crystal upon complexation of an
achiral guest molecule. Some interesting and important optical resolutions of
rac-guests by inclusion with a chiral host are
described. When chemical reaction and inclusion in a water suspension medium
are combined, new economical and ecological methods of the preparation of
optically active compounds can be established. When photochemical reactions
are performed on the guests of an inclusion-complex crystal formed with a
chiral host, enantioselective reactions occur and optically active products
can be obtained. Several successful reactions are described.
Crystalline inclusion complexes of guest compounds with various artificial
hosts are useful as media for the following molecular recognitions and
selective reactions in the solid state.
Manuscript received: 4 October 2001.
Final version: 13 November 2001.
Cited by
22 articles.
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